ClinVar Genomic variation as it relates to human health
NM_001079673.2(FNDC3A):c.3132A>G (p.Lys1044=)
Germline
Classification
(1)
Benign
no assertion criteria provided
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
FNDC3A | - | - |
GRCh38 GRCh37 |
67 | 129 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
FNDC3A-related disorder
|
Benign (1) |
|
Nov 5, 2019 | RCV003916910.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 13, 2024